Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids

Autores
Ortiz, Javier E.; Berkov, Strahil; Pigni, Natalia B.; Theoduloz, Cristina; Roitman, Gustavo Germán; Tapia, Alejandro; Bastida, Jaume; Feresin, Gabriela E.
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Fil: Roitman, Gustavo Germán. Universidad de Buenos Aires. Facultad de Agronomía. Buenos Aires, Argentina.
The Amaryllidaceae family is well known for its pharmacologically active alkaloids. An important approach to treat Alzheimer's disease involves the inhibition of the enzyme acetylcholinesterase (AChE). Galanthamine, an Amaryllidaceae alkaloid, is an effective, selective, reversible, and competitive AChE inhibitor. This work was aimed at studying the alkaloid composition of four wild Argentinian Amarillydaceae species for the first time, as well as analyzing their inhibitory activity on acetylcholinesterase. Alkaloid content was characterized by means of GC-MS analysis. Chloroform basic extracts from Habranthus jamesonii, Phycella herbertiana, Rhodophiala mendocina and Zephyranthes filifolia collected in the Argentinian Andean region all contained galanthamine, and showed a strong AChE inhibitory activity (IC 50 between 1.2 and 2 ug/mL). To our knowledge, no previous reports on alkaloid profiles and AChEIs activity of wild Argentinian Amarillydaceae species have been publisihed. The demand for renewable sources of industrial products like galanthamine and the need to protect plant biodiversity creates an opportunity for Argentinian farmers to produce such crops.
Fuente
Molecules
Vol.17, no.11
13473-13482
http://www.mdpi.com/
Materia
ACETYLCHOLINESTERASE INHIBITORS
ALKALOIDS
ARGENTINIAN AMARYLLIDACEAE WILD
GALANTHAMINE
LYCORINE
TAZETTINE
ALKALOID
CHOLINESTERASE INHIBITOR
GALANTAMINE
PLANT EXTRACT
ARGENTINA
CHEMISTRY
ISOLATION AND PURIFICATION
LILIACEAE
MASS FRAGMENTOGRAPHY
PLANT ROOT
THIN LAYER CHROMATOGRAPHY
CHOLINESTERASE INHIBITORS
CHROMATOGRAPHY, THIN LAYER
GAS CHROMATOGRAPHY-MASS SPECTROMETRY
PLANT EXTRACTS
PLANT ROOTS
Nivel de accesibilidad
acceso abierto
Condiciones de uso
acceso abierto
Repositorio
FAUBA Digital (UBA-FAUBA)
Institución
Universidad de Buenos Aires. Facultad de Agronomía
OAI Identificador
snrd:2012Ortiz

id FAUBA_849a6d0603d41f9ff278a21229e512fa
oai_identifier_str snrd:2012Ortiz
network_acronym_str FAUBA
repository_id_str 2729
network_name_str FAUBA Digital (UBA-FAUBA)
spelling Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloidsOrtiz, Javier E.Berkov, StrahilPigni, Natalia B.Theoduloz, CristinaRoitman, Gustavo GermánTapia, AlejandroBastida, JaumeFeresin, Gabriela E.ACETYLCHOLINESTERASE INHIBITORSALKALOIDSARGENTINIAN AMARYLLIDACEAE WILDGALANTHAMINELYCORINETAZETTINEALKALOIDCHOLINESTERASE INHIBITORGALANTAMINEPLANT EXTRACTARGENTINACHEMISTRYISOLATION AND PURIFICATIONLILIACEAEMASS FRAGMENTOGRAPHYPLANT ROOTTHIN LAYER CHROMATOGRAPHYCHOLINESTERASE INHIBITORSCHROMATOGRAPHY, THIN LAYERGAS CHROMATOGRAPHY-MASS SPECTROMETRYPLANT EXTRACTSPLANT ROOTSFil: Roitman, Gustavo Germán. Universidad de Buenos Aires. Facultad de Agronomía. Buenos Aires, Argentina.The Amaryllidaceae family is well known for its pharmacologically active alkaloids. An important approach to treat Alzheimer's disease involves the inhibition of the enzyme acetylcholinesterase (AChE). Galanthamine, an Amaryllidaceae alkaloid, is an effective, selective, reversible, and competitive AChE inhibitor. This work was aimed at studying the alkaloid composition of four wild Argentinian Amarillydaceae species for the first time, as well as analyzing their inhibitory activity on acetylcholinesterase. Alkaloid content was characterized by means of GC-MS analysis. Chloroform basic extracts from Habranthus jamesonii, Phycella herbertiana, Rhodophiala mendocina and Zephyranthes filifolia collected in the Argentinian Andean region all contained galanthamine, and showed a strong AChE inhibitory activity (IC 50 between 1.2 and 2 ug/mL). To our knowledge, no previous reports on alkaloid profiles and AChEIs activity of wild Argentinian Amarillydaceae species have been publisihed. The demand for renewable sources of industrial products like galanthamine and the need to protect plant biodiversity creates an opportunity for Argentinian farmers to produce such crops.2012articleinfo:eu-repo/semantics/articlepublishedVersioninfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfdoi:10.3390/molecules171113473issn:1420-3049http://ri.agro.uba.ar/greenstone3/library/collection/arti/document/2012OrtizMoleculesVol.17, no.1113473-13482http://www.mdpi.com/reponame:FAUBA Digital (UBA-FAUBA)instname:Universidad de Buenos Aires. Facultad de AgronomíaengARGinfo:eu-repo/semantics/openAccessopenAccesshttp://ri.agro.uba.ar/greenstone3/library/page/biblioteca#section42025-09-04T09:45:20Zsnrd:2012Ortizinstacron:UBA-FAUBAInstitucionalhttp://ri.agro.uba.ar/Universidad públicaNo correspondehttp://ri.agro.uba.ar/greenstone3/oaiserver?verb=ListSetsmartino@agro.uba.ar;berasa@agro.uba.ar ArgentinaNo correspondeNo correspondeNo correspondeopendoar:27292025-09-04 09:45:22.112FAUBA Digital (UBA-FAUBA) - Universidad de Buenos Aires. Facultad de Agronomíafalse
dc.title.none.fl_str_mv Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids
title Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids
spellingShingle Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids
Ortiz, Javier E.
ACETYLCHOLINESTERASE INHIBITORS
ALKALOIDS
ARGENTINIAN AMARYLLIDACEAE WILD
GALANTHAMINE
LYCORINE
TAZETTINE
ALKALOID
CHOLINESTERASE INHIBITOR
GALANTAMINE
PLANT EXTRACT
ARGENTINA
CHEMISTRY
ISOLATION AND PURIFICATION
LILIACEAE
MASS FRAGMENTOGRAPHY
PLANT ROOT
THIN LAYER CHROMATOGRAPHY
CHOLINESTERASE INHIBITORS
CHROMATOGRAPHY, THIN LAYER
GAS CHROMATOGRAPHY-MASS SPECTROMETRY
PLANT EXTRACTS
PLANT ROOTS
title_short Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids
title_full Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids
title_fullStr Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids
title_full_unstemmed Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids
title_sort Wild argentinian amaryllidaceae, a new renewable source of the acetylcholinesterase inhibitor galanthamine and other alkaloids
dc.creator.none.fl_str_mv Ortiz, Javier E.
Berkov, Strahil
Pigni, Natalia B.
Theoduloz, Cristina
Roitman, Gustavo Germán
Tapia, Alejandro
Bastida, Jaume
Feresin, Gabriela E.
author Ortiz, Javier E.
author_facet Ortiz, Javier E.
Berkov, Strahil
Pigni, Natalia B.
Theoduloz, Cristina
Roitman, Gustavo Germán
Tapia, Alejandro
Bastida, Jaume
Feresin, Gabriela E.
author_role author
author2 Berkov, Strahil
Pigni, Natalia B.
Theoduloz, Cristina
Roitman, Gustavo Germán
Tapia, Alejandro
Bastida, Jaume
Feresin, Gabriela E.
author2_role author
author
author
author
author
author
author
dc.subject.none.fl_str_mv ACETYLCHOLINESTERASE INHIBITORS
ALKALOIDS
ARGENTINIAN AMARYLLIDACEAE WILD
GALANTHAMINE
LYCORINE
TAZETTINE
ALKALOID
CHOLINESTERASE INHIBITOR
GALANTAMINE
PLANT EXTRACT
ARGENTINA
CHEMISTRY
ISOLATION AND PURIFICATION
LILIACEAE
MASS FRAGMENTOGRAPHY
PLANT ROOT
THIN LAYER CHROMATOGRAPHY
CHOLINESTERASE INHIBITORS
CHROMATOGRAPHY, THIN LAYER
GAS CHROMATOGRAPHY-MASS SPECTROMETRY
PLANT EXTRACTS
PLANT ROOTS
topic ACETYLCHOLINESTERASE INHIBITORS
ALKALOIDS
ARGENTINIAN AMARYLLIDACEAE WILD
GALANTHAMINE
LYCORINE
TAZETTINE
ALKALOID
CHOLINESTERASE INHIBITOR
GALANTAMINE
PLANT EXTRACT
ARGENTINA
CHEMISTRY
ISOLATION AND PURIFICATION
LILIACEAE
MASS FRAGMENTOGRAPHY
PLANT ROOT
THIN LAYER CHROMATOGRAPHY
CHOLINESTERASE INHIBITORS
CHROMATOGRAPHY, THIN LAYER
GAS CHROMATOGRAPHY-MASS SPECTROMETRY
PLANT EXTRACTS
PLANT ROOTS
dc.description.none.fl_txt_mv Fil: Roitman, Gustavo Germán. Universidad de Buenos Aires. Facultad de Agronomía. Buenos Aires, Argentina.
The Amaryllidaceae family is well known for its pharmacologically active alkaloids. An important approach to treat Alzheimer's disease involves the inhibition of the enzyme acetylcholinesterase (AChE). Galanthamine, an Amaryllidaceae alkaloid, is an effective, selective, reversible, and competitive AChE inhibitor. This work was aimed at studying the alkaloid composition of four wild Argentinian Amarillydaceae species for the first time, as well as analyzing their inhibitory activity on acetylcholinesterase. Alkaloid content was characterized by means of GC-MS analysis. Chloroform basic extracts from Habranthus jamesonii, Phycella herbertiana, Rhodophiala mendocina and Zephyranthes filifolia collected in the Argentinian Andean region all contained galanthamine, and showed a strong AChE inhibitory activity (IC 50 between 1.2 and 2 ug/mL). To our knowledge, no previous reports on alkaloid profiles and AChEIs activity of wild Argentinian Amarillydaceae species have been publisihed. The demand for renewable sources of industrial products like galanthamine and the need to protect plant biodiversity creates an opportunity for Argentinian farmers to produce such crops.
description Fil: Roitman, Gustavo Germán. Universidad de Buenos Aires. Facultad de Agronomía. Buenos Aires, Argentina.
publishDate 2012
dc.date.none.fl_str_mv 2012
dc.type.none.fl_str_mv article
info:eu-repo/semantics/article
publishedVersion
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv doi:10.3390/molecules171113473
issn:1420-3049
http://ri.agro.uba.ar/greenstone3/library/collection/arti/document/2012Ortiz
identifier_str_mv doi:10.3390/molecules171113473
issn:1420-3049
url http://ri.agro.uba.ar/greenstone3/library/collection/arti/document/2012Ortiz
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
openAccess
http://ri.agro.uba.ar/greenstone3/library/page/biblioteca#section4
eu_rights_str_mv openAccess
rights_invalid_str_mv openAccess
http://ri.agro.uba.ar/greenstone3/library/page/biblioteca#section4
dc.format.none.fl_str_mv application/pdf
dc.coverage.none.fl_str_mv ARG
dc.source.none.fl_str_mv Molecules
Vol.17, no.11
13473-13482
http://www.mdpi.com/
reponame:FAUBA Digital (UBA-FAUBA)
instname:Universidad de Buenos Aires. Facultad de Agronomía
reponame_str FAUBA Digital (UBA-FAUBA)
collection FAUBA Digital (UBA-FAUBA)
instname_str Universidad de Buenos Aires. Facultad de Agronomía
repository.name.fl_str_mv FAUBA Digital (UBA-FAUBA) - Universidad de Buenos Aires. Facultad de Agronomía
repository.mail.fl_str_mv martino@agro.uba.ar;berasa@agro.uba.ar
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score 12.623145